期刊
JOURNAL OF IMMUNOLOGY
卷 172, 期 8, 页码 4709-4716出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.172.8.4709
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资金
- NHLBI NIH HHS [HL46810] Funding Source: Medline
- NIAID NIH HHS [AI48602, AI41570] Funding Source: Medline
T cell diversity was once thought to depend on the interaction of T cell precursors with thymic epithelial cells. Recent evidence suggests, however, that diversity might arise through the interaction of developing T cells with other cells, the identity of which is not known. In this study we show that T cell diversity is driven by B cells and Ig. The TCR Vbeta diversity of thymocytes in mice that lack B cells and Ig is reduced to 6 x 10(2) from wild-type values of 1.1 x 10(8); in mice with oligoclonal B cells, the TCR Vbeta diversity of thymocytes is 0.01% that in wild-type mice. Adoptive transfer of diverse B cells or administration of polyclonal Ig increases thymocyte diversity in mice that lack B cells 8- and 7-fold, respectively, whereas adoptive transfer of monoclonal B cells or monoclonal Ig does not. These findings reveal a heretofore unrecognized and vital function of B cells and Ig for generation of T cell diversity and suggest a potential approach to immune reconstitution.
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